摘要
ZnCdS, a metal chalcogenide solid solution, has attracted significant attention. However, two primary challenges hinder its widespread application in photocatalytic hydrogen evolution : the rapid recombination rate of photogenerated carriers and susceptibility to photo-oxidation in the aqueous environments. In this article, a facile hydrothermal route was employed for the first time to uniformly assemble SnS 2 nanoparticles onto the surface of Zn 0.2 Cd 0.8 S (ZCS) nanopolyhedra. The intimate contact of two materials resulted in the formation of heterojunctions . By adjusting the content of SnS 2 , the hydrogen evolution reaction (HER) performance was optimized to reach up to 12170 μmol/gh, which is 1.9 times of the pristine ZCS. Notably, the photocatalyst demonstrated remarkable stability with an apparent quantum yield (AQY) of 15.5% at 420 nm. The enhanced photocatalytic performance can be attributed to the following factors: (i) The heterojunction composite, with larger surface area and more micropores, provides additional active sites and exhibits high photocatalytic activity ; (ii) The internal electric field accelerates the separation of photogenerated carriers and reduces the recombination rate of electron-hole pairs; (iii) The photogenerated holes can be quickly transferred to the valence band of SnS 2 and react with triethanolamine , thereby significantly reducing the photo-oxidation of ZCS. This work not only proposed a feasible route to improve the photocatalytic activity of ZCS, but also provided insights into the role of heterojunctions and the reaction mechanism.
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